5-BROMO-4-METHYL-PYRIDINE-2-CARBOXYLIC ACID
5-BROMO-4-METHYL-PYRIDINE-2-CARBOXYLIC ACID Basic information
- Product Name:
- 5-BROMO-4-METHYL-PYRIDINE-2-CARBOXYLIC ACID
- Synonyms:
-
- 5-Bromo-4-methylpicolinic acid, 5-Bromo-2-carboxy-4-methylpyridine
- 5-BroMo-2-carboxy-4-Methylpyridine
- 5-bromo-4-methyl-2-Pyridinecarboxylic acid
- 5-BROMO-4-METHYL-PYRIDINE-2-CARBOXYLIC ACID
- 5-broMo-4-Methylpicolinic acid
- 2-carboxylic acid-4-methyl-5-bromopyridine
- 2-Pyridinecarboxylic acid, 5-bromo-4-methyl-
- 5-bromo-4-methylpyridin-2-carboxylic acid
- CAS:
- 886365-02-2
- MF:
- C7H6BrNO2
- MW:
- 216.03
- Product Categories:
-
- Heterocycle-Pyridine series
- Mol File:
- Mol File
5-BROMO-4-METHYL-PYRIDINE-2-CARBOXYLIC ACID Chemical Properties
- Boiling point:
- 335.0±42.0 °C(Predicted)
- Density
- 1.692±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 3.48±0.10(Predicted)
- Appearance
- White to off-white Solid
5-BROMO-4-METHYL-PYRIDINE-2-CARBOXYLIC ACID Usage And Synthesis
Synthesis
1122090-37-2
886365-02-2
5-Bromo-4-methyl-2-vinylpyridine (600 mg, 3 mmol) was used as raw material and dissolved in a solvent mixture of acetone-water (1:1, 54 mL). Subsequently, potassium permanganate (KMnO4, 957 mg, 6 mmol) was added to this solution. The reaction mixture was stirred at room temperature for 3 days. Upon completion of the reaction, the mixture was filtered to remove insoluble impurities, and the filtrate was concentrated and purified by column chromatography to give 5-bromo-4-methylpyridine-2-carboxylic acid (700 mg, 92% yield) as a white solid.
References
[1] Patent: US2011/71150, 2011, A1. Location in patent: Page/Page column 33-34
[2] Patent: US2013/158040, 2013, A1. Location in patent: Paragraph 0134
[3] Patent: US2013/158049, 2013, A1. Location in patent: Paragraph 0168
[4] Patent: US2013/158066, 2013, A1. Location in patent: Paragraph 0134
[5] Patent: WO2012/143329, 2012, A1
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